A dental implant packaging container including a main body having an inner wall defining a space for receiving a dental implant, a cap detachably coupled to one side of the main body, a securing portion mounted on the cap and configured to secure the dental implant inside the main body; a bottom portion coupled to the main body and facing the cap, and a main body reflector disposed on the inner wall of the main body and reflecting UV light emitted towards the cap.

Provided is a plasma treatment apparatus that does not use a separate process gas by discharging low-pressure atmosphere formed in a sealed space in which a plasma surface treatment is performed. Therefore, by discharging the low-pressure atmosphere using a relatively low voltage, stable plasma with high surface treatment efficiency may be generated, and thus a plasma treatment apparatus may be configured economically and no operation and management costs due to the use of a process gas are incurred. Also, the safety and the effectiveness of a plasma surface treatment process to be applied in the medical industry are secured, and sterility may be secured and usability may be maximized.

A retainer for holding at least a first surgical device, preferably a dental implant, and a second surgical device, preferably a healing screw, comprising a first body part and a second body part. The first and second body parts are pivotable relative to each other, and the first body part includes a first support structure for holding the first surgical device and the retainer includes at least one secondary support structure for the second surgical device. The first and the second body parts are pivotable in relation to each other to at least three predefined positions. In a first position, the first and second surgical devices are locked in the retainer; in a second position, the first surgical device is removable from the support structure, but not the second surgical device; and in a third position, the second surgical device is removable from the retainer.

A prosthesis-packaging case (20) comprises a primary packaging case (30) for housing a prosthesis (10) and a secondary packaging case (40) for housing the primary packaging case (30), wherein the prosthesis (10) and the primary packaging case (30) are respectively made of a material containing zirconia, the secondary packaging case (40) is made of a heat-resistant material, and the prosthesis (10) is subjected to -ray sterilization treatment and heat treatment while double-packaged with the primary packaging case (30) and secondary packaging case (40) to change a color of the prosthesis (10) to a color approximate to that of a natural bone.

A package for an object includes a support element with means for coupling the object to the support element. A first hollow protective element is provided as a stopper coupled to the support element of the object. The support element presents a grip portion which projects from the stopper, the support element, alone or in co-operation with the stopper, defining a first chamber containing the object. A second hollow protective element is provided as a cover. The cover is coupled to the stopper so as to cooperate with the stopper to define a second chamber inside which the grip portion of the support element extends. The cover is coupled to the stopper, with the grip portion of the stopper projecting from the cover. The means for coupling is configured to hold the object suspended through the means for coupling, so that the object extends into the space left free between the means for coupling and a bottom portion of the support element. The bottom portion is coupled to the stopper so that the length of the object remain visible.

An implant is provided with an upper portion in which an internal socket extends. The implant can be tightened by a turning instrument which has first lateral surfaces that can cooperate with corresponding second lateral surfaces in the internal socket. One or more of the first and/or second lateral surfaces is/are arranged completely or partially with friction-enhancing means. The implant and the tool are arranged with interacting parts which extend beyond the first and second lateral surfaces and completely or substantially take up bending moments which act in or on said portion or are directed toward said portion and occur in the event of skewing, or a tendency toward skewing, between the implant and the tool. The arrangement counteracts mechanical stresses in said portion, the latter being able to retain its original shape even in the case of implants with small dimensions.

Apparatus and method for installing a multi-tooth dental prosthesis in one session are shown and described. A first tool attaches to the jawbone, and serves as a foundation for subsequently used guides. Existing teeth and dental fixtures are removed, and the bone tissue is removed to accommodate the prosthesis. Subsequently, a drill guide is used to drill implant holes. An abutment guide is then used to place abutments. Copings are then installed. Next, the prosthesis may be installed and cemented to the copings. A resinous filler material may be applied to fill gaps and holes in and between the copings and the prosthesis, and is sanded smooth.

Embodiments of the present invention provide an osseointegrative implant and related tools, components and fabrication techniques for surgical bone fixation and dental restoration purposes. In one embodiment an all-ceramic single-stage threaded or press-fit implant is provided having finely detailed surface features formed by ceramic injection molding and/or spark plasma sintering of a powder compact or green body comprising finely powdered zirconia. In another embodiment a two-stage threaded implant is provided having an exterior shell or body formed substantially entirely of ceramic and/or CNT-reinforced ceramic composite material. The implant may include one or more frictionally anisotropic bone-engaging surfaces. In another embodiment a densely sintered ceramic implant is provided wherein, prior to sintering, the porous debound green body is exposed to ions and/or particles of silver, gold, titanium, zirconia, YSZ, ?-tricalcium phosphate, hydroxyapatite, carbon, carbon nanotubes, and/or other particles which remain lodged in the implant surface after sintering. Optionally, at least the supragingival portions of an all-ceramic implant are configured to have high translucence in the visible light range. Optionally, at least the bone-engaging portions of an all-ceramic implant are coated with a fused layer of titanium oxide.

A process for the preparation of a sterilized ceramic body including or essentially consisting of stabilized zirconia of a defined colour, including the steps of: providing a ceramic primary body including or essentially consisting of stabilized zirconia of a first colour A, and sterilizing the primary body using radiation sterilization whereby the primary body undergoes a colour change to a colour B. The process includes the further step of irradiating the sterilized primary body with electromagnetic radiation of at least one wavelength lying in the wavelength band ranging from 150 nm to 700 nm to induce an at least partial reversal of the colour change to obtain a colour C of the sterilized ceramic body, the colour C complying with the following requirements in the CIELAB colour space: L* being from 54 to 95, a* being from 15 to 15 and b* being from 15 to 15.

A hydrogel comprising a colloidal suspension of M.sup.I.sub.XM.sup.II.sub.YP.sub.Z two-dimensional nanocrystals in water, wherein M.sup.I is Na.sup.+ and/or Li.sup.+, M.sup.II is Mg.sup.2+ or a mixture of Mg.sup.2+ with one or more Ni.sup.2+, Zn.sup.2+, Cu.sup.2+, Fe.sup.2+ and/or Mn.sup.2+, P is a mixture of dibasic phosphate ions (HPO.sub.4.sup.2) and tribasic phosphate ions (PO.sub.4.sup.3), X ranges from about 0.43 to about 0.63, Y ranges from about 0.10 to about 0.18, Z ranges from about 0.29 to about 0.48, X, Y, Z being mole fractions, is provided.